Canonical Allele Identifier: CA99411499

Gene: DCK MOB1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70996957T>C , CM000666.2:g.70996957T>C	GRCh38
NC_000004.11:g.71862674T>C , CM000666.1:g.71862674T>C	GRCh37
NC_000004.10:g.72081538T>C	NCBI36
NG_023303.1:g.8410T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286648.10:c.92-1110T>C (DCK) MANE Select	ENSP00000286648.5:n.92-1110T>C
ENST00000286648.9:c.92-1110T>C (DCK)	ENSP00000286648.5:n.92-1110T>C
ENST00000503359.5:c.*36-1110T>C (DCK)	ENSP00000426389.1:n.*36-1110T>C
ENST00000504730.5:c.92-1110T>C (DCK)	ENSP00000425578.1:n.92-1110T>C
ENST00000504952.1:c.92-1110T>C (DCK)	ENSP00000421508.1:n.92-1110T>C
ENST00000511449.1:n.429-1110T>C (MOB1B)
NM_000788.2:c.92-1110T>C (DCK)	NP_000779.1:n.92-1110T>C
NM_000788.3:c.92-1110T>C (DCK) MANE Select	NP_000779.1:n.92-1110T>C